N-(4-bromophenyl)-2-iodoacetamide

Base Information

Chemical Name:N-(4-bromophenyl)-2-iodoacetamide
CAS No.:17641-04-2
Molecular Formula:C8H7BrINO
Molecular Weight:339.958
Hs Code.:2924299090
NSC Number:151224
UNII:PHR8V58CAZ
DSSTox Substance ID:DTXSID10170127
Nikkaji Number:J54.141I
Wikidata:Q83039988
Mol file:17641-04-2.mol

Synonyms:N-(4-bromophenyl)-2-iodoacetamide;17641-04-2;ACETANILIDE, 4'-BROMO-2-IODO-;4'-Bromo-2-iodoacetanilide;Acetamide, N-(4-bromophenyl)-2-iodo-;PHR8V58CAZ;NSC 151224;BRN 2832521;NSC-151224;WLN: I1VMR DE;NSC151224;C8H7BrINO;UNII-PHR8V58CAZ;SCHEMBL5597893;DTXSID10170127;ACETANILIDE,4-BROMO-2-IODO-;AKOS014116754

Suppliers and Price of N-(4-bromophenyl)-2-iodoacetamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
N-(4-Bromophenyl)-2-iodoacetamide 95+%
10g
$ 972.00

Crysdot
N-(4-Bromophenyl)-2-iodoacetamide 95+%
5g
$ 748.00

American Custom Chemicals Corporation
4'-BROMO-2-IODOACETANILIDE 95.00%
5MG
$ 500.29

Total 5 raw suppliers

Chemical Property of N-(4-bromophenyl)-2-iodoacetamide

Chemical Property:

Vapor Pressure:3.11E-07mmHg at 25°C
Boiling Point:419.1°Cat760mmHg
Flash Point:207.3°C
PSA：29.10000
Density:2.158g/cm³
LogP:2.89560
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:338.87557
Heavy Atom Count:12
Complexity:157

Purity/Quality:

99.5% ^*data from raw suppliers

N-(4-Bromophenyl)-2-iodoacetamide 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1NC(=O)CI)Br

Technology Process of N-(4-bromophenyl)-2-iodoacetamide

There total 3 articles about N-(4-bromophenyl)-2-iodoacetamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

: 2564-02-5
N-(4-bromophenyl)-2-chloroacetamide

: 17641-04-2
N-(4-bromophenyl)-2-iodoacetamide

Guidance literature:: With potassium iodide; In acetone; for 8h; Reflux;
DOI:10.1002/ardp.200800107

Reference yield:

: 106-40-1
4-bromo-aniline

: 17641-04-2
N-(4-bromophenyl)-2-iodoacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 12 h / 0 - 20 °C

2: potassium iodide / acetone / 6 h / Reflux

With triethylamine; potassium iodide; In dichloromethane; acetone;
DOI:10.1016/j.tetlet.2020.151873